Canonical Allele Identifier: CA2618282095
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40298298del , CM000674.2:g.40298298del GRCh38
NC_000012.11:g.40692100del , CM000674.1:g.40692100del GRCh37
NC_000012.10:g.38978367del NCBI36
NG_011709.1:g.78288del

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.3152del MANE Select ENSP00000298910.7:p.Pro1051LeufsTer5
ENST00000679360.1:c.*2061del ENSP00000505368.1:n.*2061del
ENST00000680790.1:c.2897del ENSP00000505335.1:p.Pro966LeufsTer5
ENST00000298910.11:c.3152del ENSP00000298910.7:p.Pro1051LeufsTer5
ENST00000343742.6:c.3152del ENSP00000341930.2:p.Pro1051LeufsTer5
ENST00000430804.5:c.196del
NM_198578.3:c.3152del NP_940980.3:p.Pro1051LeufsTer5
XM_005268629.2:c.3152del XP_005268686.1:p.Pro1051LeufsTer5
XM_011537877.1:c.3152del XP_011536179.1:p.Pro1051LeufsTer5
XM_011537878.1:c.3152del XP_011536180.1:p.Pro1051LeufsTer5
XM_011537879.1:c.1949del XP_011536181.1:p.Pro650LeufsTer5
XM_011537880.1:c.3152del XP_011536182.1:p.Pro1051LeufsTer5
XM_011537881.1:c.3152del XP_011536183.1:p.Pro1051LeufsTer5
XM_011537882.1:c.3152del XP_011536184.1:p.Pro1051LeufsTer5
XM_005268629.4:c.3152del XP_005268686.1:p.Pro1051LeufsTer5
XM_011537877.3:c.3152del XP_011536179.1:p.Pro1051LeufsTer5
XM_011537881.3:c.3152del XP_011536183.1:p.Pro1051LeufsTer5
XM_011537882.3:c.3152del XP_011536184.1:p.Pro1051LeufsTer5
XM_017018786.2:c.3152del XP_016874275.1:p.Pro1051LeufsTer5
XM_017018787.1:c.68del XP_016874276.1:p.Pro23LeufsTer5
XM_017018789.2:c.3152del XP_016874278.1:p.Pro1051LeufsTer5
XM_024448833.1:c.1949del XP_024304601.1:p.Pro650LeufsTer5
XR_001748574.2:n.3394del
NM_198578.4:c.3152del MANE Select NP_940980.4:p.Pro1051LeufsTer5